Canonical Allele Identifier: CA1737344377
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797971085
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479920G>A , CM000669.2:g.117479920G>A GRCh38
NC_000007.13:g.117119974G>A , CM000669.1:g.117119974G>A GRCh37
NC_000007.12:g.116907210G>A NCBI36
NG_016465.4:g.19137G>A , LRG_663:g.19137G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-191+226G>A ENSP00000417012.1:n.-191+226G>A
ENST00000673785.1:c.-406+14089G>A ENSP00000501235.1:n.-406+14089G>A
ENST00000446805.1:c.-191+226G>A ENSP00000417012.1:n.-191+226G>A
ENST00000546407.1:n.166+4112G>A
XM_011515751.1:c.143+575G>A XP_011514053.1:n.143+575G>A
XM_011515752.1:c.143+575G>A XP_011514054.1:n.143+575G>A
XM_011515753.1:c.-191+226G>A XP_011514055.1:n.-191+226G>A
XM_011515754.1:c.-519+226G>A XP_011514056.1:n.-519+226G>A
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